
Celiprolol hydrochloride
CAS No. 57470-78-7
Celiprolol hydrochloride ( Corliprol | NSC 324509 )
产品货号. M15097 CAS No. 57470-78-7
一种心脏选择性 β1 肾上腺素能拮抗剂,具有内在的拟交感神经活性。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
100MG | 获取报价 | 有现货 |
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200MG | 获取报价 | 有现货 |
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500MG | 获取报价 | 有现货 |
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1G | 获取报价 | 有现货 |
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生物学信息
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产品名称Celiprolol hydrochloride
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述一种心脏选择性 β1 肾上腺素能拮抗剂,具有内在的拟交感神经活性。
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产品描述A cardioselective beta-1 adrenergic antagonist that has intrinsic symopathomimetic activity.
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体外实验Celiprolol hydrochloride (0-3 mM, 90 min) is uptaken by human small intestinal transporter OATP-A/1A2 in Xenopus Laevis oocytes.Celiprolol hydrochloride (10 μM, 0-50 min) is transported across human intestinal epithelial (Caco-2) cells by mediation of multiple transporters including P-glycoprotein.
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体内实验Celiprolol hydrochloride (Oral administration, 100 mg/kg/day for 31 days) improves endothelial function in the arteries of in Otsuka Long-Evans Tokushima Fatty (OLETF) rats, and restores it 4 weeks after endothelial denudation in the arteries of OLETF rats.Celiprolol hydrochloride (Treated in drinking water, 10 mg/kg/day for 5 weeks) suppresses VCAM-1 expression by inhibition of oxidative stress, NF-κB, signal transduction, and increases eNOS via stimulation of the PI3K-Akt pathway, and improves cardiovascular remodeling in deoxycorticosterone acetate (DOCA)-salt hypertensive rats. Animal Model:Type II male Otsuka Long-Evans Tokushima Fatty (OLETF) diabetic rats Dosage:100 mg/kg/day for 31 days Administration:Oral administration Result:Improved acetylcholine-induced NO-dependent relaxation in arteries.Improved tone-related basal NO release and acetylcholine-induced NO-dependent relaxation in the arteries and plasma NOx.Animal Model:Deoxycorticosterone acetate (DOCA)-salt hypertensive rats Dosage:10 mg/kg/d for 5 weeks Administration:Treated in drinking water Result:Activated phosphorylation of eNOS through the PI3K-Akt signaling pathway.Modulated VCAM-1 expression, which is associated with inhibition of NF-κB phosphorylation.Reduced production of ROS by suppressing NAD(P)H oxidase subunit p22phox, p47phox, gp91phox, and nox1 expression.
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同义词Corliprol | NSC 324509
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通路Endocrinology/Hormones
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靶点Adrenergic Receptor
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受体β-adrenergic receptor
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研究领域——
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适应症——
化学信息
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CAS Number57470-78-7
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分子量415.96
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分子式C20H33N3O4·HCl
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纯度>98% (HPLC)
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溶解度DMSO: 10 mM
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SMILESCl.CCN(CC)C(=O)NC1=CC(C(C)=O)=C(OCC(O)CNC(C)(C)C)C=C1
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1.Abdelkrim MA, et al. Can J Physiol Pharmacol. 2013 Oct;91(10):791-6.
产品手册




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